Variant report

Variant	rs6787044
Chromosome Location	chr3:90129439-90129440
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 101 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs11128081	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11917293	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11918512	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11920640	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11924267	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12106840	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12107978	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12107987	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1402829	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1402830	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1402831	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1521801	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1521805	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1915788	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1996783	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1996784	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2204078	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2204079	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55719953	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs55726199	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56257056	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs57237979	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58442773	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58444511	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs58944054	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58977999	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6551449	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs6770945	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6772724	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6780268	0.94[AFR][1000 genomes]
rs6782153	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6789752	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs6793888	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6798554	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6800191	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6800705	0.89[AFR][1000 genomes]
rs6804358	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs72921836	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs72921847	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72921850	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72921853	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72921855	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs72921864	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72921866	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72921873	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72921876	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923735	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923736	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923737	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923739	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923741	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923755	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923757	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923762	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923764	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923765	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923767	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923768	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923770	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923771	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923776	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923777	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923779	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923781	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923783	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923784	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923786	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72923794	0.90[AFR][1000 genomes]
rs73846008	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73849912	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7610765	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7619437	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7626330	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7627792	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7637541	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7648089	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7648275	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7648900	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs939741	0.94[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008018	chr3:89382031-90254063	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv536639	chr3:89382031-90254063	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1010932	chr3:89424428-90192503	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1010021	chr3:89521983-90141988	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv530024	chr3:89548440-90304841	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1008130	chr3:89837442-90192503	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1010796	chr3:89870548-90192503	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1013598	chr3:89879377-90192503	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv536642	chr3:89879377-90192503	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv590966	chr3:89904882-90199759	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1007523	chr3:89951855-90144385	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv1011581	chr3:89951855-90144746	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv997583	chr3:89951855-90154534	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv1006665	chr3:89958844-90162193	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv998541	chr3:89961515-90153365	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv536643	chr3:89961515-90153365	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	nsv590967	chr3:89979895-90138312	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	nsv590968	chr3:89979895-90199759	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
19	nsv460761	chr3:89987871-90138312	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
20	nsv590969	chr3:89987871-90138312	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
21	nsv590970	chr3:89987871-90441306	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
22	nsv1010292	chr3:90057464-90192503	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:90119800-90130200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr3:90128200-90130000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:90128800-90130000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr3:90128800-90132200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr3:90129000-90130800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr3:90129200-90130400	Weak transcription	H9 Cell Line	embryonic stem cell

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